ライフサイエンスコーパス: metatherian

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1 bles insights into the innovative biology of metatherians.

2 s), or as an outgroup to both eutherians and metatherians.

3 The new evidence supports metatherian affinities for deltatheroidans and allows a

4 Metatherian and eutherian (placental) mammals are more c

5 ic mammalian lineages of Mesozoic origin and metatherian and eutherian lineages that probably dispers

6 nter for the diversification of the earliest metatherians and eutherians during the Early Cretaceous.

7 ence of these genes before the separation of metatherians and eutherians more than 100 million years

8 comprehensive phylogenetic analysis of basal metatherians and marsupials.

9 part of a Late Cretaceous diversification of metatherians, and later dispersed to South America.

10 order of events is the same in eutherian and metatherian animals, but there is a curvilinear relation

11 d female recombination might be a widespread metatherian attribute.

12 nd high G+C contents in comparison with both metatherian autosomes and eutherian chromosomes.

13 nation in marsupials as a consequence of the metatherian characteristic of determinate paternal X chr

14 n mammal (node-based clade of eutherians and metatherians), Didelphodon vorax has a high estimated bi

15 ed that Golem originated after the eutherian-metatherian divergence and that the A and B subfamilies

16 enins were refined structurally prior to the metatherian/eutherian divergence between 100 and 150 mil

17 rsupial AAV that circulated among Australian metatherian fauna sometime during the late Eocene to ear

18 Marsupial mammal relatives (stem metatherians) from the Mesozoic Era (252-66 million year

19 Ark blot analysis of eutherian and metatherian genomic DNA indicates that X-Y homologues ar

20 suggest that it has a closer relationship to metatherians (including extant marsupials) than to euthe

21 The slowing of late developmental events in metatherians is associated with their considerably longe

22 ion between the event scales of the two; for metatherians, later events are slowed relative to earlie

23 nymous sites, to have been duplicated in the metatherian lineage.

24 Deltatheroidans are primitive metatherian mammals (relatives of marsupials), previousl

25 ession in genital tubercles of eutherian and metatherian mammals, but not turtles or alligators, indi

26 rom both the unique phylogenetic position of metatherian (marsupial) mammals and the fundamental biol

27 Like eutherians, metatherian (marsupial) mammals have evolved high CpG su

28 s, macaques, several rodent species, and six metatherian (marsupial) mammals.

29 ologs exist at the syntenic genomic locus in metatherian (marsupial) or prototherian (monotreme) mamm

30 As the first metatherian ('marsupial') species to be sequenced, the o

31 inclusive of all living placentals, from the metatherian-marsupial clade.

32 malian subgroup, with two notable exceptions-metatherians (marsupials) and euarchontans (primates and

33 Xist is not found in metatherians (marsupials), and how X-chromosome inactiva

34 nes endorsing either therian or specifically metatherian relationships.

35 mmals is here extended to an additional five metatherian species and to a variety of other events in

36 the fundamental biologic characteristics of metatherians that distinguish them from other mammalian

37 identified variously as eutherians, as basal metatherians (the stem-based clade formed by marsupials

38 remains of a North American Late Cretaceous metatherian, the stagodontid Didelphodon vorax.

39 Furthermore, in metatherians, the timing of developmental events is more

40 cula (an Australian marsupial), we show that metatherian X chromosomes have elevated silent substitut

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